Project Grant R21AI174041
- Federal Project Grant Award Summary The National Center for Advancing Translational Sciences (NCATS, CFDA 93.350) awarded $155,000 to the Regents of the University of Minnesota on September 5, 2025, to conduct secondary analyses of clinical trial data aimed at advancing understanding of Long COVID. The project, which extends through August 31, 2027, leverages the COVID-OUT trial—a Phase 3, randomized, placebo-controlled clinical trial examining early outpatient treatment of COVID-19 using...
- The Department of the Army Medical Command awarded a $1,093,692.71 Project Grant to HMH Hospitals Corporation, doing business as Hackensack University Medical Center, to support a randomized clinical study of convalescent plasma from recovered COVID-19 donors collected through plasmapheresis as treatment for early COVID-19 infection. The study aims to evaluate the safety and efficacy of convalescent plasma as a treatment option for COVID-19 under the Military Medical Research and Development...
- OPTIMIZE Lung-HIV Project Grant Summary The National Institutes of Health (NIH) Office of the Director awarded $1,557,602 through the Trans-NIH Research Support program (CFDA 93.310) on August 15, 2025, to the Seattle Institute for Biomedical and Clinical Research to develop and test a pharmacist-led proactive electronic consultation (e-consult) intervention designed to improve lung health outcomes for people with HIV (PWH). The project addresses community-acquired pneumonia as a significant...
- The National Heart, Lung, and Blood Institute (NHLBI) awarded a $2.98 million Project Grant (CFDA 93.837 – Cardiovascular Diseases Research) to the University of California, San Francisco to conduct a four-year research study examining the impact of asymptomatic cytomegalovirus (CMV) infection on cardiovascular event risk in people with HIV (PWH). The primary deliverable is a large-scale Mendelian randomization study that will assess whether CMV-associated plasma proteomic signatures and...
- MISTR+ Study: Telehealth PrEP Initiation and Retention Outcomes Emory University received a $1.27 million Project Grant from the National Institute of Allergy and Infectious Diseases (NIAID) under the Allergy and Infectious Diseases Research program (CFDA 93.855), awarded June 2, 2026, with completion targeted for May 31, 2031. The MISTR+ study will develop and test evidence-based, low-touch interventions designed to improve human immunodeficiency virus (HIV) pre-exposure prophylaxis (PrEP)...
- Federal Cooperative Agreement Summary The National Institute of Allergy and Infectious Diseases (NIAID) awarded Boston Children's Hospital a Cooperative Agreement valued at $1.67 million under the Allergy and Infectious Diseases Research program (CFDA 93.855) to conduct a Phase 1 clinical study of a novel messenger ribonucleic acid (mRNA)-based severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine. The research, initiated September 25, 2025, and scheduled for completion by July...
- Summary Albert Einstein College of Medicine received a $231,000 Project Grant from the National Institute of Allergy and Infectious Diseases (NIAID) under the Allergy and Infectious Diseases Research program (CFDA 93.855), awarded June 1, 2026, with a completion date of May 31, 2028. The grant supports research and development of human monoclonal antibodies (MAbs) designed to treat and prevent Herpes Simplex Virus (HSV) infections, including genital and neonatal herpes. Rather than pursuing...
- Federal Grant Award Summary The National Institute of Allergy and Infectious Diseases (NIAID) awarded a $463,615 Project Grant to the Regents of the University of California, San Francisco on August 6, 2025, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to investigate virologic failure and drug resistance among people with HIV (PWH) receiving long-acting antiretroviral therapy (LA-ART). The VIOLA study, spanning through July 31, 2027, addresses an emerging clinical...
- The University of Texas Health Science Center at San Antonio received a $234,715 Project Grant from the National Institute of Allergy and Infectious Diseases (NIAID) under the Allergy and Infectious Diseases Research program (CFDA 93.855), awarded February 13, 2026, with completion by January 31, 2028. The grant funds research investigating lymphotoxin beta receptor (LTBR) signaling in sensory neurons as a potential therapeutic target for managing neurological complications associated with...
- Federal Grant Award Summary New York University School of Medicine received a $836,484 Project Grant award from the National Institute of Allergy and Infectious Diseases (NIAID) under the Allergy and Infectious Diseases Research program (CFDA 93.855), effective May 19, 2026 through April 30, 2031. The award supports development of vectored immunoprophylaxis (VIP) therapeutics utilizing receptor decoy technology to protect against and treat SARS-CoV-2 infection across viral variants. The research...
ORAL ANTIVIRALS AGAINST COVID-19 AND CLINICAL OUTCOMES IN HIGH RISK POPULATIONS - COVID-19 HAS LED TO OVER 350 MILLION REPORTED CASES AND OVER 5.6 MILLION RESULTING DEATHS GLOBALLY, AND NEARLY 72 MILLION CASES AND >900,000 DEATHS IN THE US. HIGHLY EFFECTIVE VACCINES ARE NOW AVAILABLE AND ARE THE FIRST LINE OF DEFENSE. HOWEVER, IMMUNITY WANES OFF OVER TIME AND BREAKTHROUGH INFECTIONS IN FULLY VACCINATED PERSONS HAVE BEEN REPORTED, PARTICULARLY WITH THE NEWER VARIANTS. IN DECEMBER 2021, TWO NOVEL ORAL ANTIVIRAL AGENTS, NIRMATRELVIR/RITONAVIR (NMV/R) AND MOLNUPIRAVIR (MPV), WERE GRANTED EMERGENCY USE AUTHORIZATION (EUA) BY THE FDA FOR TREATMENT OF EARLY SYMPTOMATIC PATIENTS WITH MILD TO MODERATE COVID-19 AT HIGH RISK OF PROGRESSION TO SEVERE DISEASE. THESE AUTHORIZATIONS WERE GRANTED BASED ON LIMITED PUBLISHED DATA, AND CRITICAL QUESTIONS ABOUT THEIR COMPARATIVE EFFECTIVENESS, EFFECTIVENESS IN THE REAL-WORLD SETTINGS, AND EFFECTIVENESS IN SPECIFIC HIGH-RISK SUB-POPULATIONS REMAIN TO BE ANSWERED. THERE IS AN URGENT NEED TO UNDERSTAND THE REAL-WORLD EFFECTIVENESS OF THESE DRUGS, ESPECIALLY IN THE HIGH-RISK AND VULNERABLE POPULATIONS, AS WELL AS LONGER TERM CLINICAL OUTCOMES IN TREATED PATIENTS. SUCH KNOWLEDGE IS ESSENTIAL FOR THE PATIENTS, PROVIDERS, PAYORS, AND POLICYMAKERS, TO ENSURE THAT THEY ARE USED ONLY IN THE APPROPRIATE POPULATIONS AND SITUATIONS BASED ON STRONG CLINICAL EVIDENCE. TO ADDRESS THESE CRITICAL GAPS IN KNOWLEDGE, WE PROPOSE THE FOLLOWING HYPOTHESES: HYPOTHESIS 1: TREATMENT WITH NMV/R OR MPV WILL BE ASSOCIATED WITH A SIGNIFICANT REDUCTION IN COVID-19 RELATED HOSPITALIZATION AND 30-DAY ALL-CAUSE MORTALITY IN OLDER PERSONS, THOSE WITH A HIGH COMORBIDITY BURDEN, AND IN SOCIALLY VULNERABLE PERSONS. HYPOTHESIS 2: WE HYPOTHESIZE THAT NMV/R AND MPV TREATMENT WILL BE ASSOCIATED WITH A SIGNIFICANT REDUCTION IN SUBSEQUENT HOSPITAL ADMISSIONS, EMERGENCY DEPARTMENT VISITS, AND OUTPATIENT CLINIC VISITS OVER A 1-YEAR PERIOD AFTER RECOVERY. TREATMENT WILL ALSO BE ASSOCIATED WITH A LOWER INCIDENCE OF ACUTE MYOCARDIAL INFARCTION, STROKE, DECLINE IN RENAL FUNCTION, AND DIABETES, COMPARED WITH PROPENSITY-SCORE MATCHED UNTREATED PERSONS. WE WILL USE THE DEPARTMENT OF VETERANS AFFAIRS' COVID-19 SHARED DATA RESOURCE (VA ORDCOVID) WHICH CONTAINS EXTENSIVE DEMOGRAPHIC, CLINICAL, PHARMACOLOGIC, LABORATORY, VITAL SIGNS AND CLINICAL OUTCOMES INFORMATION DERIVED FROM MULTIPLE VALIDATED SOURCES. WE WILL COMPARE THOSE TREATED WITH NMV/R OR MPV WITH PROPENSITY-SCORE MATCHED UNTREATED CONTROLS, MATCHED ON DEMOGRAPHICS, CLINICAL VARIABLES, SEVERITY OF PRESENTING ILLNESS, GEOGRAPHIC LOCATION, TIME OF TREATMENT, VACCINATION STATUS, TIME FROM COMPLETION OF A FULL COURSE OF VACCINATION, AND BOOSTER DOSE ADMINISTRATION. THE PI, DR. BUTT HAS EXTENSIVE EXPERIENCE IN CREATING AND ANALYSING LARGE NATIONAL DATABASES AND HAS PUBLISHED 45 PAPERS ON COVID-19 IN JOURNALS INCLUDING THE NEW ENGLAND JOURNAL OF MEDICINE, ANNALS OF INTERNAL MEDICINE, JAMA INTERNAL MEDICINE, JOURNAL OF CLINICAL INVESTIGATION, NATURE MEDICINE, AND OTHERS. HE ALREADY HAS IRB APPROVAL TO STUDY THE EPIDEMIOLOGY, NATURAL HISTORY, AND CLINICAL OUTCOMES OF SARS-COV-2 INFECTION IN THE VA POPULATION.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $0 | 7/10/25 | ||
| Not listed | $189.4k | 7/1/24 | ||
| Not listed | $157.8k | 7/12/23 | ||
| Not listed | $157.8k | 7/12/23 |